This post was originally featured on my former blog site in 2018. A version of this post has been published on The Mighty and Yahoo News!
Becoming my authentic self, one day at a time.
At 24.5 years old, I’ve been officially diagnosed as having Autism Spectrum Disorder or ASD. I get to join the ranks of Steve Jobs, Albert Einstein, Mozart, Susan Boyle, Bill Gates(presumably) and more.
Well, can I say I’m surprised? A little. But I decided it would be best to talk about it on this blog now as it may play a crucial role in my social and academic life in Nigeria. I had originally deleted a similar post out of shame and fear that the wrong people might find this blog, but as I got to know and love myself a little more over the past few months, I realized how little that actually matters. I am proud of the person I am today and the obstacles I have overcome with this disability-and I hope to spread awareness and understanding to others.Besides, I would also love to inspire other future Fulbrighters with disabilities to apply! Additionally, although everyone on the spectrum is different, I thought it might be useful to share some of my experiences and behaviors that I’ve picked up on myself in hindsight.
The tests
I had originally decided to get tested for Autism after doing several online screenings. I had my therapist do a short professional screening, and she discovered (not me- I knew this) that I had a strong aversion to loud sounds, bright lights, and wearing certain fabric of clothing (jeans & leggings are the absolute worst, for example!). I then went to a specialist and underwent a battery of neuropsychological evaluations for a total of 5 hours over a span of 2 sessions. The evaluations tested my verbal, nonverbal reasoning, processing speed, and a few other mental health screenings that tested for depression, schizophrenia, anxiety and more. My parents were also interviewed to see how I was like as a child.
I scored mostly average to slightly above average on the majority of the tests. I also definitely have anxiety according to the BECK screening, which was completely unsurprising.
Additionally, I scored well below average in the social and nonverbal reasoning aspects of the test, but what surprised me is that it turns out my processing speed is incredibly below average. This means that I’m simply not as “quick” as most people. I’ve noticed this in social settings as I have a hard time keeping up with the pace of conversations, and I often end up not saying anything at all as a result. It’s also been a big problem for me in tests, although I just assumed everyone struggled to finish their tests on time. It might be why I’m not doing so well on the math section of the GRE (see “about me” section).
These days, autism is rated as mild, moderate or severe. With mild being the part of the spectrum for what used to be called aspergers. To my surprise, my rating is considered moderate. Which basically means that my symptoms are generally worse than people who would identify as having aspergers or high functioning autism. Given how “normal” I sometimes appear to others, it means that I unfortunately do an impressive job of masking my symptoms in social situations. However, the examiner said that since I am able to live and work on my own, I should consider myself to have what is now called high functioning autism-even though my symptoms are more severe.
My Social Life
The report said that my social affect is very flat, meaning that I often have a blank stare and do not utilize the extent of my vocabulary when talking. My parents had also told the administrator that I sometimes had a hard time picking up with mood changes when growing up, and I honestly wouldn’t be surprised if I still do now. I also have a very rigid social life. For now, it means that I join meetup groups in my select interest (bible study, running clubs and book clubs) and very rarely deviate outside of that friend group.
I also have a pretty easy time making friends, but struggle to keep them. This has gone on since middle school, but I starkly remember horrible altercations I’ve had with friends, roommates, and teammates in college and in my early twenties.
What this means for me:
Once again, everyone on the spectrum is different. But I wanted to highlight some of my experiences that are congruent with traits in people with autism:
What’s next:
The administrator mentioned that it may be useful for me to get special accommodation on tests at Oxford and my next school due to my anxiety and processing speed results. This will be a very interesting change as I don’t have to take tests in a certain time limit or have nearly as many distractions as I’ve had in the past.
It makes me wonder how I was able to solidify a high GPA in college, be an elite athlete, secure kick ass jobs and get into the best university and fellowship in the world… it’s truly a blessing and I guess the sky’s now the limit for what I can do now with an even playing field!
It also explains why applying to places has been my “thing” lately. It’s competitive and I love it. People with autism usually have a special interest in something, and this must be mine. This application cycle I’ll be applying to the Gates Cambridge Scholarship, Stanford’s Knight-Hennesy fellowship and grad school applications. This new “thing” of mine will come in handy as I progress more into my career as an aspiring University President, as applying to grants and such will be routine.
….Well, as an African American women, I can fully attest to the research that claims that late diagnosis is common in women, and even more common in African Americans. This is unfortunate because early intervention is the key to living a healthy and fulfilling life. Being diagnosed as an adult will come with a lot of challenges, but it has also already come with a lot of clarity. I find that I’m able to understand myself better, and be kinder to myself when I struggle with minor social situations. I’m hoping the future will continue to bring in more clarity and self-compassion.